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Leptospira Infection Interferes with the Prothrombinase Complex Assembly during Experimental Leptospirosis
Leptospirosis is a worldwide zoonotic and neglected infectious disease of human and veterinary concern, caused by pathogenic Leptospira species. Although bleeding is a common symptom of severe leptospirosis, the cause of hemorrhage is not completely understood. In severe infections, modulation of he...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5368274/ https://www.ncbi.nlm.nih.gov/pubmed/28400758 http://dx.doi.org/10.3389/fmicb.2017.00500 |
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author | Vieira, Monica L. de Andrade, Sonia A. Morais, Zenaide M. Vasconcellos, Silvio A. Dagli, Maria Lucia Z. Nascimento, Ana Lucia T. O. |
author_facet | Vieira, Monica L. de Andrade, Sonia A. Morais, Zenaide M. Vasconcellos, Silvio A. Dagli, Maria Lucia Z. Nascimento, Ana Lucia T. O. |
author_sort | Vieira, Monica L. |
collection | PubMed |
description | Leptospirosis is a worldwide zoonotic and neglected infectious disease of human and veterinary concern, caused by pathogenic Leptospira species. Although bleeding is a common symptom of severe leptospirosis, the cause of hemorrhage is not completely understood. In severe infections, modulation of hemostasis by pathogens is an important virulence mechanism, and hemostatic impairments such as coagulation/fibrinolysis dysfunction are frequently observed. Here, we analyze the coagulation status of experimentally infected hamsters in an attempt to determine coagulation interferences and the origin of leptospirosis hemorrhagic symptomatology. Hamsters were experimentally infected with L. interrogans. The lungs, kidneys, and livers were collected for culture, histopathology, and coagulation assays. L. interrogans infection disturbs normal coagulation in the organs of animals. Our results suggest the presence of a thrombin-like factor or FX activator, which is able to activate FII in the leptospirosis organ extracts. The activity of those factors is accelerated in the prothrombinase complex. Additionally, we show for the first time that live leptospires act as a surface for the prothrombinase complex assembly. Our results contribute to the understanding of leptospirosis pathophysiological mechanisms and may open new routes for the discovery of novel treatments in the severe manifestations of the disease. |
format | Online Article Text |
id | pubmed-5368274 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53682742017-04-11 Leptospira Infection Interferes with the Prothrombinase Complex Assembly during Experimental Leptospirosis Vieira, Monica L. de Andrade, Sonia A. Morais, Zenaide M. Vasconcellos, Silvio A. Dagli, Maria Lucia Z. Nascimento, Ana Lucia T. O. Front Microbiol Microbiology Leptospirosis is a worldwide zoonotic and neglected infectious disease of human and veterinary concern, caused by pathogenic Leptospira species. Although bleeding is a common symptom of severe leptospirosis, the cause of hemorrhage is not completely understood. In severe infections, modulation of hemostasis by pathogens is an important virulence mechanism, and hemostatic impairments such as coagulation/fibrinolysis dysfunction are frequently observed. Here, we analyze the coagulation status of experimentally infected hamsters in an attempt to determine coagulation interferences and the origin of leptospirosis hemorrhagic symptomatology. Hamsters were experimentally infected with L. interrogans. The lungs, kidneys, and livers were collected for culture, histopathology, and coagulation assays. L. interrogans infection disturbs normal coagulation in the organs of animals. Our results suggest the presence of a thrombin-like factor or FX activator, which is able to activate FII in the leptospirosis organ extracts. The activity of those factors is accelerated in the prothrombinase complex. Additionally, we show for the first time that live leptospires act as a surface for the prothrombinase complex assembly. Our results contribute to the understanding of leptospirosis pathophysiological mechanisms and may open new routes for the discovery of novel treatments in the severe manifestations of the disease. Frontiers Media S.A. 2017-03-28 /pmc/articles/PMC5368274/ /pubmed/28400758 http://dx.doi.org/10.3389/fmicb.2017.00500 Text en Copyright © 2017 Vieira, de Andrade, Morais, Vasconcellos, Dagli and Nascimento. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Vieira, Monica L. de Andrade, Sonia A. Morais, Zenaide M. Vasconcellos, Silvio A. Dagli, Maria Lucia Z. Nascimento, Ana Lucia T. O. Leptospira Infection Interferes with the Prothrombinase Complex Assembly during Experimental Leptospirosis |
title | Leptospira Infection Interferes with the Prothrombinase Complex Assembly during Experimental Leptospirosis |
title_full | Leptospira Infection Interferes with the Prothrombinase Complex Assembly during Experimental Leptospirosis |
title_fullStr | Leptospira Infection Interferes with the Prothrombinase Complex Assembly during Experimental Leptospirosis |
title_full_unstemmed | Leptospira Infection Interferes with the Prothrombinase Complex Assembly during Experimental Leptospirosis |
title_short | Leptospira Infection Interferes with the Prothrombinase Complex Assembly during Experimental Leptospirosis |
title_sort | leptospira infection interferes with the prothrombinase complex assembly during experimental leptospirosis |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5368274/ https://www.ncbi.nlm.nih.gov/pubmed/28400758 http://dx.doi.org/10.3389/fmicb.2017.00500 |
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